Canonical Allele Identifier: CA1752388567
Gene: AOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861348_150861349delinsAC , CM000669.2:g.150861348_150861349delinsAC GRCh38
NC_000007.13:g.150558436_150558437delinsAC , CM000669.1:g.150558436_150558437delinsAC GRCh37
NC_000007.12:g.150189369_150189370delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*139_*140delinsAC MANE Select ENSP00000354193.4:n.*139_*140delinsAC
ENST00000360937.8:c.*139_*140delinsAC ENSP00000354193.4:n.*139_*140delinsAC
ENST00000467291.5:c.*139_*140delinsAC ENSP00000418328.1:n.*139_*140delinsAC
ENST00000493429.5:c.*139_*140delinsAC ENSP00000418614.1:n.*139_*140delinsAC
XR_928169.1:n.295+15660_295+15661delinsGT
XR_928170.1:n.425+7267_425+7268delinsGT
XR_928171.1:n.297+15660_297+15661delinsGT
XR_928169.2:n.301+15660_301+15661delinsGT
XR_928171.2:n.301+15660_301+15661delinsGT
NM_001091.4:c.*139_*140delinsAC MANE Select NP_001082.2:n.*139_*140delinsAC
NM_001272072.2:c.*139_*140delinsAC NP_001259001.1:n.*139_*140delinsAC